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276 results on '"Colacicco, A. M."'

1. Alcohol Consumption in Predementia and Dementia Syndromes

Author

Panza, Francesco, Frisardi, Vincenza, Kehoe, Patrick G., Capurso, Cristiano, D’Introno, Alessia, Colacicco, Anna M., Vendemiale, Gianluigi, Capurso, Antonio, Solfrizzi, Vincenzo, Preedy, Victor R., editor, Watson, Ronald Ross, editor, and Martin, Colin R., editor

Published
2011
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2. Dietary Fatty Acids, Cognitive Decline, and Dementia

Author

Solfrizzi, Vincenzo, Frisardi, Vincenza, Capurso, Cristiano, D’Introno, Alessia, Colacicco, Anna M., Vendemiale, Gianluigi, Capurso, Antonio, Panza, Francesco, Preedy, Victor R., editor, Watson, Ronald Ross, editor, and Martin, Colin R., editor

Published
2011
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4. Inactivation: an opportunity for a major logistics training event: inactivating the 4th Infantry Brigade Combat Team, 1st Infantry Division, provided unique training opportunities for logisticians and allowed the unit to become a force multiplier for deploying units

Author

Colacicco, Joseph M.

Subjects
United States. Army. 1st Infantry Division -- Training, United States. Army -- Training, Deployment (Strategy), Infantry, General interest, Military and naval science
Abstract

In June 2014, the 4th Infantry Brigade Combat Team, 1st Infantry Division (ID) (4/1 IBCT), received formal notice that it was to begin inactivation as part of force restructuring. The [...]

Published
2016

15. The cathepsin D gene exon 2 (C224T) polymorphism and sporadic Alzheimer's disease in European populations

Author

Capurso, Cristiano, Solfrizzi, Vincenzo, D'Introno, Alessia, Colacicco, Anna M., Capurso, Sabrina A., Mastroianni, Franco, Liaci, Maria, Vendemiale, Gianluigi, Capurso, Antonio, and Panza, Francesco

Subjects
Alzheimer's disease -- Genetic aspects, Alzheimer's disease -- Research, Genetic polymorphisms, Gene mutations, Genetic research, Health, Seniors
Abstract

The cathepsin D gene (CTSD) exon 2 (C224T) polymorphism has been associated with an increased risk for sporadic Alzheimer's disease (AD), but with controversial findings. We studied CTSD exon 2 (C224T) and apolipoprotein E (APOE) genotype frequencies in 168 AD patients and 218 age-matched healthy controls from Southern Italy. No statistically significant differences were found in CTSD allele or genotype frequencies between AD patients and controls, and there were no interactions with sex or APOE genotype. Furthermore, comparing our results with the findings from other European populations, the CTSD*T allele frequency showed a statistically significant increasing trend from Northern to Southern regions of Europe in AD patients and controls (z = 2.51, p < .01; z = 4.02, p < .001, respectively), with a concomitant inverse trend for CTSD*C allele frequency. The regional differences in CTSD allele frequencies could be related to the different patterns of association between this polymorphism and AD in various European studies.

Published
2005

16. Polymorphisms in the oxidized low-density lipoprotein receptor-1 gene and risk of Alzheimer's disease

Author

D'Introno, Alessia, Solfrizzi, Vincenzo, Colacicco, Anna M., Capurso, Cristiano, Torres, Francesco, Capurso, Sabrina A., Capurso, Antonio, and Panza, Francesco

Subjects
Alzheimer's disease, Gene mutations, Genetic research, Health, Seniors
Abstract

The +1073 C/T polymorphism of the oxidized low-density lipoprotein receptor-1 (OLR1) gene has been reported to be associated with late-onset Alzheimer's disease, whereas for the +1071 T/A polymorphism no association was found. We genotyped 169 sporadic Alzheimer's disease patients and 264 sex- and age-matched nondemented controls from Southern Italy for OLRI +1073 C/T and +1071 T/A polymorphisms and for apolipoprotein E and LBP-1c/CP2/LSF. We also performed haplotype analysis. For the +1073 C/T polymorphism, the C allele and the CC genotype have been associated with a higher risk for Alzheimer's disease without apolipoprotein E or CP2 interaction. The two polymorphisms were in linkage disequilibrium, with the haplotype T-C at significant increased risk of developing Alzheimer's disease in the whole sample and in elderly persons 70 years or older. In our population, the +1073 C/T OLR1 polymorphism exhibited a significant association with Alzheimer's disease, further supporting the role of OLRI as a candidate risk gene for sporadic Alzheimer's disease.

Published
2005

26. Molecular Determinants of Human Longevity

Author

Panza, Francesco, primary, D'Introno, Alessia, additional, Colacicco, Anna M., additional, Capurso, Cristiano, additional, Palasciano, Rosa, additional, Capurso, Sabrina, additional, Gadaleta, Annamaria, additional, Capurso, Antonio, additional, Kehoe, Patrick G., additional, and Solfrizzi, Vincenzo, additional

Published
2005
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